Comparison Table
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| TruSeq RNA Access | SMARTer Ultra Low RNA | NEW! TruSight RNA Pan-Cancer Panel | TruSight RNA Fusion | SureCell WTA 3′ Library Prep Kit | |
|---|---|---|---|---|---|
| Intended Use | Clearest, most complete view of the coding transcriptome with precise strand information in both high and low-quality samples. | Robust analysis of the coding transcriptome down to single cell input levels in high-quality samples. Used with Nextera XT. | Comprehensive assessment of cancer-related RNA transcripts enabling detection of gene fusions, variants, and gene expression changes in all cancer types. | Gene fusion detection with known and novel partners in 507 fusion associated genes. Simplified analysis solution reports all detected fusions. | Single cell RNA sequencing. This kit provides a validated process for single-cell RNA sequencing allowing for the quick isolation and barcoding of ~1200 cells per cartridge from multiple sources using Bio-Rad droplet generator and a quick and easy library preparation using Illumina's Nextera XT kits. |
| Input Amount | 10ng High Quality Total RNA 20ng Degraded Total RNA |
10pg-10ng Total RNA | 10 ng for high quality RNA 20–100 ng for FFPE RNA |
10 ng for high quality RNA 20–100 ng for FFPE RNA |
45,000 cells per cartridge |
| FFPE Compatible | Yes | No | Yes | Yes | No |
| Multiplexing | 1–24 | 1–384 | 1–24 | 1–24 | 1–24 |
| Capture Method | Probes targeting coding RNA sequence | Oligo dT priming to create cDNA | Enrichment | Enrichment | Oligo dT capture, single cell |
| Capture Content | Coding Transcriptome | Coding Transcriptome | 1385 cancer related genes | 507 cancer related genes | 3′ enriched coding transcriptome |
| Stranded | Yes | No | Yes | Yes | Yes |